Principal Clinical Research Scientist

Danaher Corp

Not specified
Master's or doctoral degree in life sciences
7+ years clinical research experience
Global clinical study design and execution
Danaher Corp, through its subsidiary Radiometer, seeks a Principal Clinical Research Scientist to lead the clinical evidence strategy for its diagnostic portfolio. The role demands strong scientific leadership and a deep understanding of clinical study design while promoting a culture of innovation and collaboration

Job Summary

  • The Principal Clinical Research Scientist will provide scientific leadership for the design and execution of global clinical studies supporting Radiometer's diagnostic portfolio.
  • This role requires strong strategic thinking to shape clinical evidence strategies for regulatory approval and lifecycle management of new medical products.
  • Radiometer offers a culture of belonging where diverse ideas are celebrated and continuous improvement drives tangible impact on patient care.

Matching Summary

Match Score: 85

Danaher Corp, through its subsidiary Radiometer, seeks a Principal Clinical Research Scientist to lead the clinical evidence strategy for its diagnostic portfolio. The role demands strong scientific leadership and a deep understanding of clinical study design while promoting a culture of innovation and collaboration.

Skills & Requirements

Must-have

  • Master's or Doctoral degree in Life Sciences
  • 7+ years clinical research experience
  • Global clinical study design and execution
  • FDA and IVDR regulatory compliance knowledge
  • Scientific writing and data interpretation skills

Nice-to-have

  • Experience with Blood Gas systems
  • Point of Care diagnostics background
  • KOL and KEE collaboration experience
  • Danaher Business System familiarity
  • Cross-functional influence in matrix organization

Key Requirements

  • Master's degree with 7+ years experience OR Doctoral degree with 5+ years
  • Solid understanding of GCP, FDA, and IVDR regulations
  • Proven ability to lead regulatory interactions and submissions
  • High proficiency in scientific writing and critical data review

Work Rights

Not specified

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